Polypeptide extracted from nematocyst venom of fire medusa and application thereof
A technology of fire jellyfish thorns and venom, applied in the field of polypeptides, can solve the problems of difficulty in separation and purification of jellyfish toxins, difficulty in the separation and purification of toxins, and achieve the effect of fewer separation steps, rapid separation, and mild separation conditions
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Embodiment 1
[0042] A polypeptide molecule, the amino acid sequence of which is shown in SEQ ID No.1;
[0043] SEQ ID No. 1:
[0044]
[0045]
Embodiment 2
[0047] The extraction of the polypeptide of the present invention:
[0048] Step 1. Take the tentacles from the live fire jellyfish and mix them with deionized water at 0°C in a volume ratio of 1:1. After stirring and standing still, take the precipitate and repeat it twice. Centrifuge for the first time. The centrifugation conditions are: centrifugal force 1000G, 4°C, 15min, collect the precipitate;
[0049] Step 2. Mix the precipitate obtained in step 1 with the disodium hydrogen phosphate-sodium dihydrogen phosphate buffer solution with a total phosphate concentration of 0.025mol / L and a pH of 5.5 according to the mass volume ratio of 1g: 40mL, and ultrasonically crush it for the second time. Centrifuge, the centrifugation conditions are: centrifugal force 13000G, 4°C, 2h, collect the supernatant to obtain the venom protein;
[0050] Step 3, take the venom protein obtained in step 2, dilute it 3 times with a buffer solution of disodium hydrogen phosphate-sodium dihydrogen ...
Embodiment 3
[0054] The extraction of the polypeptide of the present invention:
[0055] Step 1. Take the tentacles from the live fire jellyfish and mix them with deionized water at 4°C at a volume ratio of 1:1.5. After stirring and standing still, take the precipitate and repeat it for 4 times. Centrifuge for the first time. The centrifugation conditions are: centrifugal force 1000G, 4°C, 15min, collect the precipitate;
[0056] Step 2, mix the precipitate obtained in step 1 with the disodium hydrogen phosphate-sodium dihydrogen phosphate buffer solution with a total phosphate concentration of 0.025mol / L and a pH of 6.5 according to the mass volume ratio of 1g: 60mL, and ultrasonically crush it for the second time Centrifuge, the centrifugation conditions are: centrifugal force 13000G, 4°C, 2h, collect the supernatant to obtain the venom protein;
[0057] Step 3, take the venom protein obtained in step 2, dilute it 5 times with the disodium hydrogen phosphate-sodium dihydrogen phosphate ...
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